JPH01280723A - Liquid crystal element - Google Patents
Liquid crystal elementInfo
- Publication number
- JPH01280723A JPH01280723A JP7917288A JP7917288A JPH01280723A JP H01280723 A JPH01280723 A JP H01280723A JP 7917288 A JP7917288 A JP 7917288A JP 7917288 A JP7917288 A JP 7917288A JP H01280723 A JPH01280723 A JP H01280723A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- ferroelectric liquid
- substrates
- alignment
- state
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 48
- 239000005262 ferroelectric liquid crystals (FLCs) Substances 0.000 claims abstract description 35
- 239000000758 substrate Substances 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 229920000642 polymer Polymers 0.000 claims abstract description 9
- 229920000106 Liquid crystal polymer Polymers 0.000 claims description 11
- 230000007704 transition Effects 0.000 claims description 4
- -1 especially Substances 0.000 abstract description 13
- 239000004990 Smectic liquid crystal Substances 0.000 abstract description 6
- 229920001296 polysiloxane Polymers 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 230000007423 decrease Effects 0.000 abstract description 3
- 238000007789 sealing Methods 0.000 abstract description 3
- 230000002093 peripheral effect Effects 0.000 abstract 1
- 229920000058 polyacrylate Polymers 0.000 abstract 1
- 239000010408 film Substances 0.000 description 32
- 239000002585 base Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000004642 Polyimide Substances 0.000 description 7
- 229920001721 polyimide Polymers 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 238000004528 spin coating Methods 0.000 description 6
- 239000011521 glass Substances 0.000 description 5
- 125000006850 spacer group Chemical group 0.000 description 5
- 229920000297 Rayon Polymers 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229920000620 organic polymer Polymers 0.000 description 4
- 239000002964 rayon Substances 0.000 description 4
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 239000002262 Schiff base Substances 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000015654 memory Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 150000004753 Schiff bases Chemical group 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000001405 butyl (E)-3-phenylprop-2-enoate Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 230000003189 isokinetic effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は、表示素子、ライトバルブ、光シヤツター、光
メモリーなどの用途を有する液晶素子に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to a liquid crystal element that has uses such as display elements, light valves, optical shutters, and optical memories.
強誘電性液晶を用いた液晶表示素子、液晶シャッター、
液晶ライトバルブ、光情報処理用スイッチング素子、光
メモリーなどの液晶素子では、液晶を一方向に優先的に
配向させる必要がある。この配向処理はこれらの液晶素
子の品質に大きな影響を与えることから多くの研究がな
されている。Liquid crystal display elements using ferroelectric liquid crystals, liquid crystal shutters,
In liquid crystal elements such as liquid crystal light valves, switching elements for optical information processing, and optical memories, it is necessary to preferentially align liquid crystal in one direction. Since this alignment treatment has a great influence on the quality of these liquid crystal elements, much research has been conducted on it.
液晶の基板表面での配向状態には、基板面に平行に配向
するホモジニアス配向と、基板面に垂直に配向するホメ
オトロピック配向とに大きくわけられる。The alignment state of liquid crystal on the substrate surface can be broadly classified into homogeneous alignment, which is aligned parallel to the substrate surface, and homeotropic alignment, which is aligned perpendicular to the substrate surface.
実際の液晶は、このように配向された強誘電性液晶に電
界などを印加することにより、液晶の配向状態を変化さ
せ、複屈折、2色性等を利用して、光の0N−OFFを
行う。In actual liquid crystals, by applying an electric field etc. to the ferroelectric liquid crystals oriented in this way, the alignment state of the liquid crystals is changed, and by using birefringence, dichroism, etc., light is turned on and off. conduct.
従来の液晶の配向方法としては、無機物の斜方蒸着、シ
ランカップリング剤塗膜や有機高分子塗膜のラビングな
どが知られているが、いずれも満足のいくものではない
。無機物の斜方蒸着はバッチ処理のため時間がかかり、
生産性が悪い。また、シランカップリング剤の塗膜をラ
ビングする方法は、信頼性に乏しい。さらに、有機高分
子塗膜をラビングして配向膜とする方法では、一般に耐
熱性の悪いものが多い。耐熱性が良好で広く用いられて
いるポリイミドの場合では、均質なモノドメインを得る
ことは困難であり、また駆動時のコン1−ラスト比が小
さく、更には、双安定性が悪く高速応答性が低下すると
いう難点がある。Conventional methods for aligning liquid crystals include oblique vapor deposition of inorganic materials, rubbing of silane coupling agent coatings, and rubbing of organic polymer coatings, but none of these methods are satisfactory. Oblique deposition of inorganic materials is a batch process, which takes time.
Poor productivity. Moreover, the method of rubbing the coating film of the silane coupling agent is poor in reliability. Furthermore, in the method of rubbing an organic polymer coating film to form an alignment film, many of the films generally have poor heat resistance. In the case of polyimide, which has good heat resistance and is widely used, it is difficult to obtain homogeneous monodomains, the contrast ratio during driving is low, and furthermore, it has poor bistability and high-speed response. The problem is that the value decreases.
また、一般に従来公知の強誘電性液晶は機械的強度に劣
り、衝撃力を加えると破損するといった難点を有する。Furthermore, conventionally known ferroelectric liquid crystals generally have a disadvantage that they have poor mechanical strength and break when subjected to impact force.
本発明は、特定の配向膜を用いることにより、液晶、特
に強誘電性液晶の配向性を改良し、均一なモノドメイン
状態の配向性を示すと共に駆動時のコントラス1〜比が
大きく、良好な双安定性を有し、かつ優れた機械的強度
を有する液晶素子を提供することを目的とする。The present invention improves the alignment of liquid crystals, particularly ferroelectric liquid crystals, by using a specific alignment film, exhibits uniform monodomain alignment, and has a large contrast ratio of 1 to 1 during driving, resulting in good results. An object of the present invention is to provide a liquid crystal element that has bistability and excellent mechanical strength.
本発明によれば、対向する一対の基板の内側に各々電極
及び液晶を配向させる配向層とを有し、その間に強誘電
性液晶層を設けてなる液晶素子において、配向層を形成
する成分として液晶状態を呈する温度が」二足強誘電性
液晶が等労相に転移する温度よりも高い液晶性高分子化
合物を用いたことを特徴とする液晶素子が提供される。According to the present invention, in a liquid crystal element which has an electrode and an alignment layer for aligning liquid crystal on the inside of a pair of opposing substrates, and a ferroelectric liquid crystal layer is provided between them, the component forming the alignment layer is A liquid crystal element is provided, which uses a liquid crystalline polymer compound whose temperature at which it exhibits a liquid crystal state is higher than the temperature at which a bipedal ferroelectric liquid crystal transitions to an isotonic phase.
一般に液晶の配向は配向膜の配向規制力によって行なわ
れるが、この配向規制力が強過ぎると強誘電性液晶の特
徴のひとつである双安定性を阻害し、高速応答性の低下
を招来する。Generally, the alignment of liquid crystals is carried out by the alignment regulating force of an alignment film, but if this alignment regulating force is too strong, it inhibits the bistability, which is one of the characteristics of ferroelectric liquid crystals, leading to a decrease in high-speed response.
本発明者らは、液晶として強誘電性液晶を用いたとして
も、欠陥の少ない均一なモノドメイン状態の配向が得ら
れるとともに機械的強度に優れ、しかも安定した双安定
性を示し、かつ駆動時のコンI〜ラスト比の大きい液晶
素子の研究を進めた結果、配向膜として液晶状態を呈す
る温度が強誘電性液晶が等労相に転移する温度よりも高
い液晶性高分子化合物を用いた液晶素子が」−記1■1
的に合致することを見出し、本発明を完成するに至った
。The present inventors have discovered that even if a ferroelectric liquid crystal is used as the liquid crystal, it is possible to obtain uniform monodomain alignment with few defects, have excellent mechanical strength, and exhibit stable bistability during driving. As a result of research into liquid crystal elements with a large contrast ratio, we have discovered a liquid crystal element using a liquid crystalline polymer compound whose temperature at which it exhibits a liquid crystal state as an alignment film is higher than the temperature at which ferroelectric liquid crystal transitions to an isokinetic phase. ”-Note 1■1
The present invention was completed based on the discovery that these conditions are consistent with each other.
従って、本発明の液晶素子は配向膜の主成分として液晶
状態を呈する温度が強誘電性液晶が等方相に転移する温
度よりも高い液晶性高分子化合物を用いたことを特徴と
する。Therefore, the liquid crystal element of the present invention is characterized in that a liquid crystalline polymer compound whose temperature at which it exhibits a liquid crystal state is higher than the temperature at which ferroelectric liquid crystal transitions to an isotropic phase is used as the main component of the alignment film.
このような液晶性を有する高分子化合物としては種々の
ものが挙げられるが、特に主鎖もしくは側鎖にメソーゲ
ン基を有し液晶状態においてネマティック相又はスメク
ティック相を呈する例えば(ポリアクリレ−1〜やポリ
シロキサン)等の高分子化合物の使用が好ましい。There are various kinds of polymer compounds having such liquid crystal properties, but in particular, polymer compounds having a mesogenic group in the main chain or side chain and exhibiting a nematic phase or a smectic phase in the liquid crystal state, such as (polyacrylate-1 and polyacrylate-1), The use of polymeric compounds such as siloxane) is preferred.
以下にその代表体側を示す。The representative side is shown below.
〔主鎖型のネマティック液晶性高分子化合物の例〕〔側
鎖型のネマティック液晶性高分子化合物の例〕〔主鎖型
のスメクティック液晶性高分子化合物の例〕〔側鎖型の
スメクティック液晶性高分子化合物の例〕本発明の配向
膜材を用いて基板上に配向膜を形成するには、前記液晶
性高分子化合物を蒸着、スピンコー1〜、ローラコー1
〜、スプレーコート、ディッピング等の従来公知の方法
により塗布し、ついで、溶剤除去のために加熱して、膜
厚100〜5000人、好ましくは500〜2000人
の配向膜とした後、綿布、ナイロン植毛布4ポリ工ステ
ル植毛布等によリラビンク処理あるいは斜方蒸着すれば
よい。[Example of main chain type nematic liquid crystalline polymer compound] [Example of side chain type nematic liquid crystalline polymer compound] [Example of main chain type smectic liquid crystalline polymer compound] [Side chain type smectic liquid crystalline polymer compound] Example of polymer compound] To form an alignment film on a substrate using the alignment film material of the present invention, the liquid crystalline polymer compound is vapor-deposited, spin coat 1 to roller coat 1
~, applied by a conventionally known method such as spray coating or dipping, and then heated to remove the solvent to form an alignment film with a film thickness of 100 to 5,000 layers, preferably 500 to 2,000 layers. Flocked fabric 4 Relabinc treatment or oblique vapor deposition may be performed using a polyester flocked fabric or the like.
以下、添付図面に沿って本発明の詳細な説明する。Hereinafter, the present invention will be described in detail with reference to the accompanying drawings.
第1図は、本発明の液晶素子の構成例を示す断面図であ
る。偏光板1,1の間に上基板2と下基板2とが対向し
て配設され、外周部が封止剤5でシールされ内部に強誘
電性液晶6が封入されている。FIG. 1 is a sectional view showing an example of the structure of a liquid crystal element according to the present invention. An upper substrate 2 and a lower substrate 2 are disposed facing each other between polarizing plates 1, 1, their outer peripheries are sealed with a sealant 5, and a ferroelectric liquid crystal 6 is sealed inside.
液晶としては、強誘電性液晶に2色性色素を混入したも
のも用いることができる。下基板2の表面には透明電極
3が設けられ、さらに下基板上2に配向膜4が形成され
ている。また、」二基板1の対向面しこは透明電極3が
設けられ、さらにその下に配向膜4が形成されている。As the liquid crystal, a ferroelectric liquid crystal mixed with a dichroic dye can also be used. A transparent electrode 3 is provided on the surface of the lower substrate 2, and an alignment film 4 is further formed on the upper surface 2 of the lower substrate. Further, a transparent electrode 3 is provided on the opposing surfaces of the two substrates 1, and an alignment film 4 is further formed below the transparent electrode 3.
配向膜4,4は前記液晶性高分子化合物からなり、液晶
分子は配向膜4,4に対して水平方向に配向している。The alignment films 4, 4 are made of the liquid crystalline polymer compound, and the liquid crystal molecules are aligned in the horizontal direction with respect to the alignment films 4, 4.
第2図は本発明の他の実施態様の構成例を示す。FIG. 2 shows a configuration example of another embodiment of the present invention.
この態様においては、」−基板又は/及び下基板2の表
面にまず有機高分子膜からなる下地層8を形成し、その
上に液晶高分子化合物による配向膜4が形成されている
。有機高分子膜からなる下地層8はポリイミド、ポリア
ミド、ポリビニルアルコール、ポリアクリロニ1〜リル
、シランカップリング剤などの高分子化合物の薄膜によ
って形成されたものであり、必要に応してラビング処理
を施したものである。このような下地層8を形成するこ
とにより配向膜4自体の配向性が向上し、更には強誘電
性液晶6の配向性の向」二につながる。In this embodiment, a base layer 8 made of an organic polymer film is first formed on the surface of the substrate and/or the lower substrate 2, and an alignment film 4 made of a liquid crystal polymer compound is formed thereon. The base layer 8 made of an organic polymer film is formed of a thin film of a polymer compound such as polyimide, polyamide, polyvinyl alcohol, polyacryloni-1-lyl, or a silane coupling agent, and is subjected to a rubbing treatment if necessary. This is what I did. By forming such a base layer 8, the orientation of the alignment film 4 itself is improved, and furthermore, the orientation of the ferroelectric liquid crystal 6 is improved.
このようにして形成した液晶素子しこおいては、従来公
知のラビング処理か斜方蒸着処理等の1軸配向処理より
液晶分子を1軸配向させることができる。またこの−軸
配向処理は、配向膜4,4の両方に対して行ってもよい
が、場合によっては、その一方のみに行った方が良好な
結果を与える場合がある。In the liquid crystal element thus formed, the liquid crystal molecules can be uniaxially aligned by a conventionally known uniaxial alignment treatment such as rubbing treatment or oblique evaporation treatment. Further, although this -axis alignment treatment may be performed on both of the alignment films 4, 4, in some cases, better results may be obtained when it is performed on only one of them.
本発明で用いる基板は、表面にパターン化された透明電
極を有するもので、従来公知のものが使用され、例えば
、ガラスの他、ポリエチレンテレフタレー1−、ポリブ
チレンテレフレート等のポリエステルの他、エポキシ樹
脂、フェノール樹脂、ポリイミド、ポリカーボネー1−
、ポリスルホン、ポリエーテルスルホン、ポリエーテル
イミド、アセチルセルロース、ポリアミノ酸エステル、
芳香族ポリアミド等の耐熱性樹脂、ポリスチレン、ポリ
アクリル酸エステル、ポリメタクリル酸エステル、ポリ
アクリルアミド、ポリエチレン、ポリプロピレン等のビ
ニル系ポリマー、ポリフッ化ビニリデン等の含フツ素樹
脂及びそれらの変性体等から形成されたプラスチックフ
ィルムが挙げられる。The substrate used in the present invention has a patterned transparent electrode on its surface, and conventionally known substrates are used, such as glass, polyester such as polyethylene terephthalate, polybutylene terephthalate, etc. Epoxy resin, phenolic resin, polyimide, polycarbonate 1-
, polysulfone, polyether sulfone, polyetherimide, acetylcellulose, polyamino acid ester,
Made from heat-resistant resins such as aromatic polyamides, vinyl polymers such as polystyrene, polyacrylic esters, polymethacrylic esters, polyacrylamide, polyethylene, and polypropylene, fluorine-containing resins such as polyvinylidene fluoride, and modified products thereof. Examples include plastic films made of plastic.
また、液晶としては、従来公知の強誘電性液晶材料が任
意に使用される。以下に、その具体例を示す。Further, as the liquid crystal, a conventionally known ferroelectric liquid crystal material may be optionally used. A specific example is shown below.
〔アミルアルコールを不斉源としたシップ塩基系強誘電
性液晶〕〔シッフ塩基のオルト位に水酸基を有する強誘
電性液晶〕〔ハロゲン、シアノ基を不斉炭素に有するシ
ップ塩基系強誘電性液晶〕C,o2n+、0−1O−C
I(=:N0CH−cH−cOo−C1(2−68−C
I+3r+=−4,5−8,10〔その他のシッフ塩基
系化合物〕
〔アゾおよびアゾキシ系強誘電性液晶〕Cl1H211
+l O−c>N=N−O)−()−C1,−シ;1ト
QHs n=16〔2環系強誘
電性液晶〕
H3
一011刑)1.テat(co、)2
〔アミルアルコール等を不斉源として多環系強誘電性液
晶〕〔ハロゲン、シアノ基等の環置換基を導入した強誘
電性液晶〕〔ピリミジン環を有する強誘電性液晶〕〔ア
ミノ酸を不斉源とした強誘電性液晶〕c、u2n、、a
−o−(Q)−(Q16−o−co、−4n−cH:+
+3)、 n=8−12〔実施例〕
以下、実施例により本発明を更に詳細に説明する。[Ship base-based ferroelectric liquid crystal with amyl alcohol as an asymmetric source] [Ferroelectric liquid crystal with a hydroxyl group at the ortho position of the Schiff base] [Ship base-based ferroelectric liquid crystal with a halogen or cyano group at the asymmetric carbon ]C, o2n+, 0-1O-C
I(=:N0CH-cH-cOo-C1(2-68-C
I+3r+=-4,5-8,10 [Other Schiff base compounds] [Azo and azoxy ferroelectric liquid crystal] Cl1H211
+l O−c>N=N−O)−()−C1,−C;1toQHs n=16 [Bicyclic ferroelectric liquid crystal] H3 1011) 1. at(co,)2 [Polycyclic ferroelectric liquid crystal using amyl alcohol as an asymmetric source] [Ferroelectric liquid crystal with a ring substituent such as halogen or cyano group introduced] [Ferroelectric liquid crystal with a pyrimidine ring Liquid crystal] [Ferroelectric liquid crystal using amino acids as an asymmetric source] c, u2n,, a
-o-(Q)-(Q16-o-co, -4n-cH:+
+3), n=8-12 [Example] Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1
ガラス基板上に前記一般式Cm)で示されるネマティッ
ク液晶性ポリシロキサン(n=46)の、3重量%テト
ラヒドロフラン溶液をスピンコーティングにより塗布し
、厚さ1 、00OAの配向膜を得た。配向膜表面をレ
ーヨン植毛布でラビング処理した後、粒径2.0μmの
スペーサ粒子を介して貼り合わせ、セルを作製した。こ
の中に強誘電性液晶としてチッソ■製C5−1013を
注入し、配向性を調べたところ、極めて良好であり、長
期間放置しても劣化は認められなかった。Example 1 A 3% by weight tetrahydrofuran solution of nematic liquid crystalline polysiloxane (n=46) represented by the general formula Cm) was applied onto a glass substrate by spin coating to obtain an alignment film with a thickness of 1.00 OA. . After rubbing the surface of the alignment film with a rayon flocked cloth, the films were bonded together with spacer particles having a particle size of 2.0 μm interposed therebetween to produce a cell. C5-1013 manufactured by Chisso Corporation was injected into this as a ferroelectric liquid crystal, and its orientation was examined. It was found to be extremely good, and no deterioration was observed even after being left for a long period of time.
実施例2
ガラス基板上に、日本合成ゴム■製ポリイミド溶液JI
B−1をスピンコーティングにより塗布し、厚さ約50
0人のポリイミド下地層を形成した。この表面をレーヨ
ン植毛布でラビング処理した後、前記一般式〔V〕で表
わされるネマティック液晶性ポリシロキサン(n=46
)の、3重量%トルエン溶液を同じくス
ピンコーティングによりこの上に塗布し、約1..00
0人の配向膜を形成した。次に基板を約270°Cに加
熱し、1℃/分の割合で、240℃まで徐冷して配向膜
自身を配向させた後、室温まで急冷してその状態を固定
させた。以下実施例1と同様に粒径2.0μmのスペー
サ粒子を介して貼り合わせてセルを作製し、強誘電性液
晶としてDOBAMBC(デシロキシベンジリデンアミ
ノメチルブチルシンナメート)を注入して、配向性を調
べたところ極めて良好であり、衝撃力を加えても配向の
乱れは生じなかった。Example 2 Polyimide solution JI manufactured by Japan Synthetic Rubber was placed on a glass substrate.
B-1 was applied by spin coating to a thickness of approximately 50 mm.
A polyimide base layer of 0 was formed. After rubbing this surface with a rayon flocked cloth, the nematic liquid crystalline polysiloxane represented by the general formula [V] (n=46
A 3% by weight toluene solution of 1.) was applied thereon by spin coating as well. .. 00
An alignment film was formed for 0 people. Next, the substrate was heated to about 270° C. and slowly cooled to 240° C. at a rate of 1° C./min to orient the alignment film itself, and then rapidly cooled to room temperature to fix that state. Thereafter, as in Example 1, a cell was fabricated by bonding them together via spacer particles with a particle size of 2.0 μm, and DOBAMBC (decyloxybenzylidene aminomethyl butyl cinnamate) was injected as a ferroelectric liquid crystal to improve the orientation. Upon examination, it was found to be in very good condition, and no disturbance in orientation occurred even when impact force was applied.
実施例3
ガラス基板上に前記一般式〔■〕で表わされるスメクテ
ィック液晶性ポリシロキサン(n=46)の、3重量%
テトラヒドロフラン溶液をスピンコーティングにより塗
布し、厚さ約1..000人の配向膜を得た。配向膜表
面をレーヨン植毛布でラビング処理した後、粒径2.0
μmのスペーサ粒子を介して貼り合わせ、セルを作製し
た。この中に強誘電性液晶としてチッソ■製C3−1,
01,]を注入し、配向性を調べたところ極めて良好で
あり、長期間放置しても劣化は認められなかった。Example 3 3% by weight of smectic liquid crystalline polysiloxane (n=46) represented by the above general formula [■] on a glass substrate
A tetrahydrofuran solution was applied by spin coating to a thickness of about 1. .. 000 alignment films were obtained. After rubbing the surface of the alignment film with rayon flocked cloth, the particle size was 2.0.
A cell was fabricated by bonding them together via μm spacer particles. Among these are C3-1 manufactured by Chisso Corporation as a ferroelectric liquid crystal.
01,] was injected and the orientation was examined, and it was found to be extremely good, and no deterioration was observed even after being left for a long period of time.
実施例4
ガラス基板上に、日本合成ゴム■製のポリイミド溶液J
IB−1をスピンコーティングにより塗布し、厚さ50
0人のポリイミド下地層を形成した。この表面レーヨン
植毛布でラビング処理した後、前記一般式〔■〕で示さ
れるスメクティック液晶ポリシロキサン(n=46)の
3重量%テトラヒドロフラン溶液を同じくスピンコーテ
ィングによりこの上に塗布し、約1 、000人の配向
膜を形成した。次に基板を約1.80°Cに加熱し、1
℃/分の割合で140℃まで徐冷して配向膜自身を配向
させた後、室温まで急冷してその状態を固定させた。以
下実施例1と同様に粒径2 、 Opmのスペーサ粒子
を介して貼り合せてセルに作製し、強誘電性液晶として
チッソ■製C3−]013を注入し、配向性を調べたと
ころ極めて良好であり、外部より?af撃力を加えても
配向はほとんど乱れなかった。Example 4 Polyimide solution J manufactured by Nippon Synthetic Rubber ■ was placed on a glass substrate.
IB-1 was applied by spin coating to a thickness of 50
A polyimide base layer of 0 was formed. After the surface was rubbed with rayon flocked cloth, a 3% by weight tetrahydrofuran solution of smectic liquid crystal polysiloxane (n=46) represented by the general formula [■] was applied thereon by spin coating, and the coating was applied with a coating of approximately 1,000% by weight. A human alignment film was formed. Next, heat the substrate to approximately 1.80°C and
After slowly cooling to 140°C at a rate of 140°C/min to orient the alignment film itself, it was rapidly cooled to room temperature and fixed in that state. In the same manner as in Example 1, a cell was fabricated by pasting spacer particles with a particle size of 2 Opm, and C3-]013 manufactured by Chisso Corporation was injected as a ferroelectric liquid crystal, and the orientation was examined and found to be extremely good. And from the outside? Even when AF impact force was applied, the orientation was hardly disturbed.
本発明の液晶素子は、特定の配向膜を用いたことから、
液晶特に強誘電性液晶の配向性が改良され、均一なモノ
ドメイン状態の配向性を示すとともにコン1−ラス1−
の低下がなく、高速応答性に優れ、更には機械的強度も
優れたものである。Since the liquid crystal element of the present invention uses a specific alignment film,
The alignment of liquid crystals, especially ferroelectric liquid crystals, has been improved, showing a uniform monodomain state alignment and a concentric 1-
It has excellent high-speed response without any deterioration in performance, and also has excellent mechanical strength.
第1−図及び第2図は、強誘電性液晶を用いた本発明の
液晶素子の構成例を示す断面図である。
】・・・偏光板、 2・基板、 3・透明電極、4・・
配向膜、 5・・封止剤、6・・・強誘電性液晶層、7
スペーサ、8・・下地層。1 and 2 are cross-sectional views showing an example of the structure of a liquid crystal element of the present invention using a ferroelectric liquid crystal. ]...Polarizing plate, 2.Substrate, 3.Transparent electrode, 4.
alignment film, 5... sealing agent, 6... ferroelectric liquid crystal layer, 7
Spacer, 8... Base layer.
Claims (2)
配向させる配向層とを有し、その間に強誘導電性液晶層
を設けてなる液晶素子において、配向層を形成する成分
として液晶状態を呈する温度が上記強誘電性液晶が等方
相に転移する温度よりも高い液晶性高分子化合物を用い
たことを特徴とする液晶素子。(1) In a liquid crystal element that has an electrode and an alignment layer for aligning liquid crystal on the inside of a pair of opposing substrates, and a ferroelectric liquid crystal layer is provided between them, the component forming the alignment layer is in a liquid crystal state. 1. A liquid crystal element using a liquid crystalline polymer compound which exhibits a temperature higher than a temperature at which the ferroelectric liquid crystal transitions to an isotropic phase.
られている特許請求の範囲第1項記載の液晶素子。(2) The liquid crystal element according to claim 1, wherein a base layer made of a polymer compound is provided inside the substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7917288A JPH01280723A (en) | 1988-03-31 | 1988-03-31 | Liquid crystal element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7917288A JPH01280723A (en) | 1988-03-31 | 1988-03-31 | Liquid crystal element |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01280723A true JPH01280723A (en) | 1989-11-10 |
Family
ID=13682557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7917288A Pending JPH01280723A (en) | 1988-03-31 | 1988-03-31 | Liquid crystal element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01280723A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05181141A (en) * | 1991-12-03 | 1993-07-23 | G T C:Kk | Method for controlling orientation of liquid crystal |
-
1988
- 1988-03-31 JP JP7917288A patent/JPH01280723A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05181141A (en) * | 1991-12-03 | 1993-07-23 | G T C:Kk | Method for controlling orientation of liquid crystal |
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